Phenotype #0000010370
| Individual ID |
00011683 |
| Associated disease |
GA1 |
| Inheritance |
Familial, autosomal recessive |
| Age/Onset |
00y06m |
| Diagnosis/Initial |
- |
| Age/Examination |
01y00m (1 year) |
| Diagnosis/Definite |
- |
| Age/Diagnosis |
- |
| Phenotype/Onset |
- |
| Phenotype details |
retardation, dystonia, macrocephaly |
| Protein |
- |
| Biochem |
glutarylcarnitine(blood): 0.38 µM/L (c: 0.02-0.20); 3-OH-GA(urine): 15.73 (fold change vs. normal control); GA(urine): 651.68 (fold change vs. normal control) |
| Enzyme/Activity |
- |
| Owner name |
Svenja Wagner |
| Database submission license |
No license selected |
| Created by |
Svenja Wagner |
| Date created |
2014-02-20 09:37:45 +01:00 (CET) |
| Date last edited |
2014-04-09 16:25:28 +02:00 (CEST) |
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